Run ID: SRR13861304
Sample name:
Date: 03-04-2023 09:28:34
Number of reads: 576527
Percentage reads mapped: 19.24
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5149 | c.-91G>C | upstream_gene_variant | 1.0 |
gyrB | 7090 | p.Asp617Glu | missense_variant | 1.0 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.17 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.17 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.17 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.15 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.14 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.13 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.21 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.17 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.19 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.18 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.14 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.14 |
gyrA | 7862 | c.561C>G | synonymous_variant | 0.19 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.15 |
gyrA | 7883 | c.582G>C | synonymous_variant | 0.15 |
gyrA | 7884 | p.Arg195Gly | missense_variant | 0.16 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.16 |
gyrA | 8024 | c.723T>C | synonymous_variant | 0.12 |
gyrA | 8036 | c.735A>G | synonymous_variant | 0.18 |
gyrA | 8039 | c.738T>C | synonymous_variant | 0.16 |
gyrA | 8048 | c.747C>T | synonymous_variant | 0.17 |
gyrA | 8054 | c.753T>C | synonymous_variant | 0.15 |
gyrA | 8057 | c.756A>G | synonymous_variant | 0.16 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.15 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.14 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.15 |
gyrA | 8096 | c.795T>C | synonymous_variant | 0.15 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.15 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.21 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.21 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.2 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.2 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.2 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.16 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.18 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.17 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.17 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.16 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.18 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.12 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.12 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.13 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.17 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.15 |
gyrA | 8436 | p.Tyr379Asn | missense_variant | 0.91 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.18 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.17 |
gyrA | 9281 | c.1980C>G | synonymous_variant | 0.17 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.17 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.17 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.16 |
gyrA | 9305 | c.2004C>G | synonymous_variant | 0.16 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.17 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.16 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.14 |
fgd1 | 491701 | p.His307Asn | missense_variant | 1.0 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.14 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.14 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.15 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.15 |
ccsA | 619765 | c.-126G>A | upstream_gene_variant | 1.0 |
ccsA | 620349 | c.459A>G | synonymous_variant | 0.12 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.15 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.14 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.18 |
rpoB | 762489 | p.Val895His | missense_variant | 0.15 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.15 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.16 |
rpoC | 763835 | p.Ala156Thr | missense_variant | 0.13 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.16 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.15 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.15 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.14 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.14 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.16 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.17 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.17 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.18 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.19 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.16 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.15 |
rpoC | 764530 | c.1161C>G | synonymous_variant | 0.16 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.14 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.13 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.13 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.14 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.14 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.14 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.13 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.15 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.15 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.17 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.15 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.15 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.15 |
rpoC | 767033 | p.Ser1222Thr | missense_variant | 0.14 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.23 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.24 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.24 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.22 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.19 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.21 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.19 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.19 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
mmpL5 | 775867 | p.Arg872Gly | missense_variant | 0.95 |
mmpL5 | 776710 | p.Cys591Ser | missense_variant | 1.0 |
mmpL5 | 777625 | p.Gln286Lys | missense_variant | 1.0 |
mmpS5 | 778811 | p.Phe32Ser | missense_variant | 1.0 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.14 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.18 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.2 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.22 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.22 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.18 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.18 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.19 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.19 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.2 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.25 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.33 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.23 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.23 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.25 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.25 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.23 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.14 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.16 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.14 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.14 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.15 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.15 |
embR | 1416901 | c.447G>C | synonymous_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474466 | n.810delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475224 | n.1567T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476263 | n.2606C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476589 | n.2932G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.17 |
inhA | 1673589 | c.-613A>G | upstream_gene_variant | 0.12 |
fabG1 | 1673598 | p.Lys53Asn | missense_variant | 0.12 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.14 |
PPE35 | 2170487 | c.126T>A | synonymous_variant | 1.0 |
Rv1979c | 2221853 | p.Phe438Ile | missense_variant | 1.0 |
kasA | 2518413 | p.Ser100Asn | missense_variant | 0.17 |
kasA | 2518421 | p.Val103Leu | missense_variant | 0.17 |
kasA | 2518426 | c.312T>C | synonymous_variant | 0.15 |
kasA | 2518429 | c.315A>C | synonymous_variant | 0.15 |
kasA | 2518439 | p.Ala109Ser | missense_variant | 0.15 |
kasA | 2518444 | c.330T>C | synonymous_variant | 0.15 |
kasA | 2518447 | c.333T>G | synonymous_variant | 0.18 |
kasA | 2518450 | c.336C>G | synonymous_variant | 0.18 |
kasA | 2518459 | c.345T>C | synonymous_variant | 0.18 |
kasA | 2518462 | c.348A>C | synonymous_variant | 0.18 |
kasA | 2518468 | c.354A>T | synonymous_variant | 0.21 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.21 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.21 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.21 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.23 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.23 |
kasA | 2518513 | c.399C>G | synonymous_variant | 0.25 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.29 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.25 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.28 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.21 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.21 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.21 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.23 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.36 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.33 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.29 |
kasA | 2518621 | c.507G>A | synonymous_variant | 0.33 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.29 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.26 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.24 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.17 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.17 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.15 |
ribD | 2987369 | c.531G>A | synonymous_variant | 1.0 |
thyA | 3073872 | p.Ile200Met | missense_variant | 0.14 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.14 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.15 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.15 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.19 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.2 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.19 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.27 |
thyA | 3073975 | p.Arg166Pro | missense_variant | 0.76 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.24 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.24 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.25 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.23 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.31 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.25 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.25 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.21 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.21 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.25 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.18 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.2 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.2 |
Rv3236c | 3612013 | c.1104A>T | synonymous_variant | 1.0 |
Rv3236c | 3612032 | p.Met362Arg | missense_variant | 1.0 |
fbiB | 3642560 | c.1026T>C | synonymous_variant | 0.17 |
fbiB | 3642566 | c.1032A>G | synonymous_variant | 0.16 |
fbiB | 3642581 | c.1047A>C | synonymous_variant | 0.17 |
fbiB | 3642593 | c.1059G>C | synonymous_variant | 0.15 |
fbiB | 3642602 | c.1068A>C | synonymous_variant | 0.2 |
fbiB | 3642605 | c.1071A>G | synonymous_variant | 0.2 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.26 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.26 |
fbiB | 3642656 | c.1122G>C | synonymous_variant | 0.23 |
fbiB | 3642659 | c.1125C>G | synonymous_variant | 0.23 |
fbiB | 3642662 | c.1128C>G | synonymous_variant | 0.23 |
fbiB | 3642668 | c.1134A>C | synonymous_variant | 0.24 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.23 |
fbiB | 3642680 | c.1146A>G | synonymous_variant | 0.23 |
fbiB | 3642684 | c.1150T>C | synonymous_variant | 0.23 |
fbiB | 3642694 | p.Ala387Gly | missense_variant | 0.18 |
fbiB | 3642696 | c.1162C>T | synonymous_variant | 0.19 |
fbiB | 3642701 | c.1167C>G | synonymous_variant | 0.19 |
fbiB | 3642710 | c.1176G>C | synonymous_variant | 0.19 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 0.2 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.2 |
fbiB | 3642743 | c.1209T>C | synonymous_variant | 0.2 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.12 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.17 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.2 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.18 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.19 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.21 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.24 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.21 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.21 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.2 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.15 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.16 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.17 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.17 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.16 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.21 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.17 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.17 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.15 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.17 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.18 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.17 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.17 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.16 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.15 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.16 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.16 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.15 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.19 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.18 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.21 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.25 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.17 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.17 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.16 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.16 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.16 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.14 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.15 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.17 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.16 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.15 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.17 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.17 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.17 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.17 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.18 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.23 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.17 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.17 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.17 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.17 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.14 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.14 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.17 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.17 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.17 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.17 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.17 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.16 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.16 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.15 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.16 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.13 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.14 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.14 |
embC | 4240425 | p.Arg188Pro | missense_variant | 1.0 |
embC | 4240477 | c.615C>A | synonymous_variant | 1.0 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.14 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.12 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.12 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.15 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.17 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.15 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.18 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.18 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.17 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.17 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.15 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.15 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.15 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.14 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.14 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.13 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.13 |
embA | 4244214 | p.Ala328Ser | missense_variant | 1.0 |
embA | 4244849 | c.1617C>G | synonymous_variant | 1.0 |
embA | 4245038 | c.1806C>T | synonymous_variant | 0.16 |
embA | 4245056 | c.1824C>G | synonymous_variant | 0.17 |
embA | 4245077 | c.1845G>C | synonymous_variant | 0.14 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.18 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.17 |
embB | 4245830 | c.-684G>C | upstream_gene_variant | 0.15 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.17 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.17 |
embB | 4247198 | p.Thr229Pro | missense_variant | 1.0 |
embB | 4247381 | p.Trp290Arg | missense_variant | 0.96 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.12 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.12 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.12 |
aftB | 4268115 | p.Leu241Arg | missense_variant | 1.0 |
aftB | 4268696 | c.141G>A | synonymous_variant | 1.0 |
ethA | 4326298 | c.1176G>A | synonymous_variant | 1.0 |
whiB6 | 4338567 | c.-46C>A | upstream_gene_variant | 1.0 |